Canonical Allele Identifier: CA383024439

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121393304G>T (hg19) ; chr11:g.121522595G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522595G>T , CM000673.2:g.121522595G>T	GRCh38
NC_000011.9:g.121393304G>T , CM000673.1:g.121393304G>T	GRCh37
NC_000011.8:g.120898514G>T	NCBI36
NG_023313.1:g.75344G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1414G>T MANE Select	ENSP00000260197.6:p.Gly472Cys
ENST00000260197.11:c.1414G>T	ENSP00000260197.6:p.Gly472Cys
ENST00000532451.1:n.1366G>T
NM_003105.5:c.1414G>T	NP_003096.1:p.Gly472Cys
XM_011542963.1:c.1414G>T	XP_011541265.1:p.Gly472Cys
XM_011542964.1:c.1414G>T	XP_011541266.1:p.Gly472Cys
XM_011542965.1:c.-209G>T	XP_011541267.1:n.-209G>T
XM_011542963.3:c.1414G>T	XP_011541265.1:p.Gly472Cys
XM_011542965.3:c.-209G>T	XP_011541267.1:n.-209G>T
XM_017018169.2:c.1102G>T	XP_016873658.1:p.Gly368Cys
XM_017018170.2:c.889G>T	XP_016873659.1:p.Gly297Cys
XM_017018171.1:c.1414G>T	XP_016873660.1:p.Gly472Cys
NM_003105.6:c.1414G>T MANE Select	NP_003096.2:p.Gly472Cys